A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510730



Internal ID20884052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:250945..274649hg38UCSC Ensembl
chr16:300944..324649hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3823705
hg1923706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029500
Samples
Known GenesITFG3, RGS11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510730
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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